Novel Neurocognitive Profile in a Minority of Boys with 47,XXY (Klinefelter Syndrome)

被引:2
|
作者
Samango-Sprouse, Carole A. [1 ,2 ,3 ]
Hamzik, Mary P. [3 ]
Khaksari, Kosar [3 ]
Brooks, Michaela R. [3 ]
Sadeghin, Teresa [3 ]
Gropman, Andrea L. [4 ,5 ]
机构
[1] George Washington Univ, Dept Pediat, Washington, DC 20052 USA
[2] Florida Int Univ, Dept Human & Mol Genet, Miami, FL 33199 USA
[3] Focus Fdn, Dept Res, Davidsonville, MD USA
[4] Childrens Natl Hlth Syst, Div Neurogenet & Dev Pediat, Washington, DC USA
[5] George Washington Univ, Dept Neurol, Washington, DC USA
关键词
Samango-Sprouse; Klinefelter syndrome; 47; XXY; neurodevelopment; neurocognitive profile; XXY; PREVALENCE; CHILDHOOD; PHENOTYPE; LITERACY; LANGUAGE; CHILDREN;
D O I
10.1097/DBP.0000000000001111
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Introduction:47,XXY, also known as Klinefelter syndrome, is the most commonly occurring sex chromosomal variation (1:660). The neurocognitive profile of boys with 47,XXY, in addition to verbal abilities, language skills, and general intelligence, has been explored in this study.Methods:Fifty-five participants with 47,XXY were segregated into groups according to their performance on the Wechsler Intelligence Scale for Children (WISC): (1) those with a higher performance intelligence quotient (PIQ) in comparison with their verbal IQ (VIQ) and (2) those with a higher VIQ compared with their PIQ. Two-tailed independent t tests were completed to analyze group differences.Results:Our study results demonstrate novel findings that one-third of subjects have higher verbal capabilities than perceptual skills. Those participants who showed the typical presentation of 47,XXY with increased PIQ in comparison with their VIQ excelled on perceptual and visual spatial subtests on the WISC and on nonverbal IQ on the Leiter International Performance Scale-III. In addition, it was found that expressive and receptive vocabulary skills were commensurate in both groups, which has not been reported previously.Discussion:To the best of our knowledge, this is the first study to identify an alternative profile of 47,XXY with increased verbal capabilities in comparison with perceptual skills. In addition, previous research has found that boys with 47,XXY often show increased receptive vocabulary skills in comparison with their expressive vocabulary skills early in life. Therefore, our findings of commensurate expressive and receptive vocabulary skills suggest that age may be an impactful factor in vocabulary development. Further research is necessary to determine individualized treatment options for these patients, focusing on the specific cognitive profile they present.
引用
收藏
页码:E623 / E628
页数:6
相关论文
共 50 条
  • [1] Behavioral and Social Phenotypes in Boys With 47, XYY Syndrome or 47, XXY Klinefelter Syndrome
    Ross, Judith L.
    Roeltgen, David P.
    Kushner, Harvey
    Zinn, Andrew R.
    Reiss, Allan
    Bardsley, Martha Zeger
    McCauley, Elizabeth
    Tartaglia, Nicole
    PEDIATRICS, 2012, 129 (04) : 769 - 778
  • [2] Morbidity and mortality in Klinefelter syndrome (47,XXY)
    Bojesen, Anders
    Gravholt, Claus H.
    ACTA PAEDIATRICA, 2011, 100 (06) : 807 - 813
  • [3] Early androgen deficiency in infants and young boys with 47,XXY Klinefelter syndrome
    Ross, JL
    Samango-Sprouse, C
    Lahlou, N
    Kowal, K
    Elder, FF
    Zinn, A
    HORMONE RESEARCH, 2005, 64 (01) : 39 - 45
  • [4] International investigation of neurocognitive and behavioral phenotype in 47,XXY (Klinefelter syndrome): Predicting individual differences
    Samango-Sprouse, Carole
    Stapleton, Emily
    Chea, Selena
    Lawson, Patrick
    Sadeghin, Teresa
    Cappello, Chris
    de Sonneville, Leo
    van Rijn, Sophie
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2018, 176 (04) : 877 - 885
  • [5] Neurodevelopmental outcome of prenatally diagnosed boys with 47,XXY (Klinefelter syndrome) and the potential influence of early hormonal therapy
    Samango-Sprouse, Carole A.
    Tran, Selena L.
    Lasutschinkow, Patricia C.
    Sadeghin, Teresa
    Powell, Sherida
    Mitchell, Francie L.
    Gropman, Andrea
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2020, 182 (08) : 1881 - 1889
  • [6] Update On The Clinical Perspectives And Care Of The Child With 47,XXY (Klinefelter Syndrome)
    Samango-Sprouse, Carole A.
    Counts, Debra R.
    Tran, Selena L.
    Lasutschinkow, Patricia C.
    Porter, Grace F.
    Gropman, Andrea L.
    APPLICATION OF CLINICAL GENETICS, 2019, 12 : 191 - 202
  • [7] The incidence of anxiety symptoms in boys with 47,XXY (Klinefelter syndrome) and the possible impact of timing of diagnosis and hormonal replacement therapy
    Samango-Sprouse, Carole
    Lasutschinkow, Patricia
    Powell, Sherida
    Sadeghin, Teresa
    Gropman, Andrea
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2019, 179 (03) : 423 - 428
  • [8] IMPACT OF EARLY HORMONAL TREATMENT (EHT) ON THE NEUROBEHAVIORAL PROFILE OF BOYS WITH 47,XXY (KLINEFELTER SYNDROME) AT 9 YEARS OF AGE
    Samango-Sprouse, C.
    Stapleton, E.
    Sadeghin, T.
    Gibbs, D. C.
    Gropman, A. L.
    JOURNAL OF INTELLECTUAL DISABILITY RESEARCH, 2014, 58 (10) : 887 - 888
  • [9] AN EXTRA X OR Y CHROMOSOME: CONTRASTING THE COGNITIVE AND MOTOR PHENOTYPES IN CHILDHOOD IN BOYS WITH 47,XYY SYNDROME OR 47,XXY KLINEFELTER SYNDROME
    Ross, Judith L.
    Zeger, Martha P. D.
    Kushner, Harvey
    Zinn, Andrew R.
    Roeltgen, David P.
    DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS, 2009, 15 (04) : 309 - 317
  • [10] Emotion regulation in adults with Klinefelter syndrome (47,XXY): Neurocognitive underpinnings and associations with mental health problems
    van Rijn, Sophie
    Swaab, Hanna
    JOURNAL OF CLINICAL PSYCHOLOGY, 2020, 76 (01) : 228 - 238